Canonical Allele Identifier: CA2753331141

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178593101_178593102insCACACCCAACAC , CM000664.2:g.178593101_178593102insCACACCCAACAC	GRCh38
NC_000002.11:g.179457828_179457829insCACACCCAACAC , CM000664.1:g.179457828_179457829insCACACCCAACAC	GRCh37
NC_000002.10:g.179166074_179166075insCACACCCAACAC	NCBI36
NG_011618.3:g.242701_242702insGTGTTGGGTGTG , LRG_391:g.242701_242702insGTGTTGGGTGTG
NG_051363.1:g.75275_75276insCACACCCAACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.51332-19_51332-18insGTGTTGGGTGTG (TTN)	ENSP00000343764.6:n.51332-19_51332-18insGTGTTGGGTGTG
ENST00000342175.11:c.32417-19_32417-18insGTGTTGGGTGTG (TTN)	ENSP00000340554.6:n.32417-19_32417-18insGTGTTGGGTGTG
ENST00000359218.10:c.32216-19_32216-18insGTGTTGGGTGTG (TTN)	ENSP00000352154.5:n.32216-19_32216-18insGTGTTGGGTGTG
ENST00000342175.10:c.32417-19_32417-18insGTGTTGGGTGTG (TTN)	ENSP00000340554.6:n.32417-19_32417-18insGTGTTGGGTGTG
ENST00000342992.10:c.51332-19_51332-18insGTGTTGGGTGTG (TTN)	ENSP00000343764.6:n.51332-19_51332-18insGTGTTGGGTGTG
ENST00000359218.9:c.32216-19_32216-18insGTGTTGGGTGTG (TTN)	ENSP00000352154.5:n.32216-19_32216-18insGTGTTGGGTGTG
ENST00000460472.6:c.31841-19_31841-18insGTGTTGGGTGTG (TTN)	ENSP00000434586.1:n.31841-19_31841-18insGTGTTGGGTGTG
ENST00000589042.5:c.59036-19_59036-18insGTGTTGGGTGTG (TTN) MANE Select	ENSP00000467141.1:n.59036-19_59036-18insGTGTTGGGTGTG
ENST00000591111.5:c.54113-19_54113-18insGTGTTGGGTGTG (TTN)	ENSP00000465570.1:n.54113-19_54113-18insGTGTTGGGTGTG
ENST00000615779.4:c.54113-19_54113-18insGTGTTGGGTGTG (TTN)	ENSP00000483597.1:n.54113-19_54113-18insGTGTTGGGTGTG
NM_001256850.1:c.54113-19_54113-18insGTGTTGGGTGTG (TTN)	NP_001243779.1:n.54113-19_54113-18insGTGTTGGGTGTG
NM_001267550.2:c.59036-19_59036-18insGTGTTGGGTGTG (TTN) MANE Select	NP_001254479.2:n.59036-19_59036-18insGTGTTGGGTGTG
NM_003319.4:c.31841-19_31841-18insGTGTTGGGTGTG (TTN)	NP_003310.4:n.31841-19_31841-18insGTGTTGGGTGTG
NM_133378.4:c.51332-19_51332-18insGTGTTGGGTGTG (TTN)	NP_596869.4:n.51332-19_51332-18insGTGTTGGGTGTG
NM_133432.3:c.32216-19_32216-18insGTGTTGGGTGTG (TTN)	NP_597676.3:n.32216-19_32216-18insGTGTTGGGTGTG
NM_133437.4:c.32417-19_32417-18insGTGTTGGGTGTG (TTN)	NP_597681.4:n.32417-19_32417-18insGTGTTGGGTGTG
NR_038271.1:n.597-4495_597-4494insCACACCCAACAC (TTN-AS1)
NR_038272.1:n.3364+1787_3364+1788insCACACCCAACAC (TTN-AS1)
XM_011511729.1:c.58133-19_58133-18insGTGTTGGGTGTG (TTN)	XP_011510031.1:n.58133-19_58133-18insGTGTTGGGTGTG
XM_011511730.1:c.32027-19_32027-18insGTGTTGGGTGTG (TTN)	XP_011510032.1:n.32027-19_32027-18insGTGTTGGGTGTG
XM_011511731.1:c.31886-19_31886-18insGTGTTGGGTGTG (TTN)	XP_011510033.1:n.31886-19_31886-18insGTGTTGGGTGTG
XM_017004819.1:c.57929-19_57929-18insGTGTTGGGTGTG (TTN)	XP_016860308.1:n.57929-19_57929-18insGTGTTGGGTGTG
XM_017004820.1:c.53327-19_53327-18insGTGTTGGGTGTG (TTN)	XP_016860309.1:n.53327-19_53327-18insGTGTTGGGTGTG
XM_017004821.1:c.53324-19_53324-18insGTGTTGGGTGTG (TTN)	XP_016860310.1:n.53324-19_53324-18insGTGTTGGGTGTG
XM_017004822.1:c.50366-19_50366-18insGTGTTGGGTGTG (TTN)	XP_016860311.1:n.50366-19_50366-18insGTGTTGGGTGTG
XM_017004823.1:c.31982-19_31982-18insGTGTTGGGTGTG (TTN)	XP_016860312.1:n.31982-19_31982-18insGTGTTGGGTGTG
XM_024453094.1:c.53477-19_53477-18insGTGTTGGGTGTG (TTN)	XP_024308862.1:n.53477-19_53477-18insGTGTTGGGTGTG
XM_024453095.1:c.53474-19_53474-18insGTGTTGGGTGTG (TTN)	XP_024308863.1:n.53474-19_53474-18insGTGTTGGGTGTG
XM_024453096.1:c.52907-19_52907-18insGTGTTGGGTGTG (TTN)	XP_024308864.1:n.52907-19_52907-18insGTGTTGGGTGTG
XM_024453097.1:c.50249-19_50249-18insGTGTTGGGTGTG (TTN)	XP_024308865.1:n.50249-19_50249-18insGTGTTGGGTGTG
XM_024453098.1:c.50168-19_50168-18insGTGTTGGGTGTG (TTN)	XP_024308866.1:n.50168-19_50168-18insGTGTTGGGTGTG
XM_024453099.1:c.31931-19_31931-18insGTGTTGGGTGTG (TTN)	XP_024308867.1:n.31931-19_31931-18insGTGTTGGGTGTG
XM_024453100.1:c.21785-19_21785-18insGTGTTGGGTGTG (TTN)	XP_024308868.1:n.21785-19_21785-18insGTGTTGGGTGTG